ENST00000261609.13:c.11880T>C
MANE Select
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ENSP00000261609.8:p.Asn3960=
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ENST00000650509.1:c.3591T>C
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ENSP00000496936.1:p.Asn1197=
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|
ENST00000261609.11:c.11880T>C
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ENSP00000261609.7:p.Asn3960=
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NM_004667.5:c.11880T>C
|
NP_004658.3:p.Asn3960=
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|
XM_005268276.3:c.11766T>C
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XP_005268333.1:p.Asn3922=
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XM_005268277.3:c.11766T>C
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XP_005268334.1:p.Asn3922=
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XM_006720726.2:c.11865T>C
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XP_006720789.1:p.Asn3955=
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XM_006720727.2:c.11622T>C
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XP_006720790.1:p.Asn3874=
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|
XM_011522131.1:c.11397T>C
|
XP_011520433.1:p.Asn3799=
|
|
XM_011522132.1:c.9396T>C
|
XP_011520434.1:p.Asn3132=
|
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XM_011522133.1:c.8625T>C
|
XP_011520435.1:p.Asn2875=
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XM_011522134.1:c.5997T>C
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XP_011520436.1:p.Asn1999=
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|
XM_005268276.5:c.11766T>C
|
XP_005268333.1:p.Asn3922=
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|
XM_006720726.3:c.11865T>C
|
XP_006720789.1:p.Asn3955=
|
|
XM_006720727.3:c.11622T>C
|
XP_006720790.1:p.Asn3874=
|
|
XM_017022695.1:c.11766T>C
|
XP_016878184.1:p.Asn3922=
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XM_017022696.1:c.11766T>C
|
XP_016878185.1:p.Asn3922=
|
|
XM_017022697.1:c.5046T>C
|
XP_016878186.1:p.Asn1682=
|
|
XM_017022698.1:c.5046T>C
|
XP_016878187.1:p.Asn1682=
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|
NM_004667.6:c.11880T>C
MANE Select
|
NP_004658.3:p.Asn3960=
|
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